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Nov. 28 - Validation Documentation Requirements and Responsibilities for Drug Fabricators, Packagers / Labellers, Testers, Distributors and Importers

Posted Date: 
Monday, November 28, 2005

A new version of the document entitled "Validation Documentation Requirements and Responsibilities for Drug Fabricators, Packagers / Labellers, Testers, Distributors and Importers" is now available. This document has been reviewed as part of the Inspectorate's quality management process and has been amended to further clarify issues brought to the attention of the Inspectorate.

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Nexreg’s dynamic staff has been a welcoming partnership in helping us keep abreast of all regulatory changes for both our Canadian and European operations, including local translation to meet the demand of our world markets. We really appreciate their product knowledge, solid customer service and attentiveness to our ever changing business needs.
Ken. L. Watt, Kleen-flo Tumbler Industries Ltd.